WO2007088114A1 - Préparation stabilisante pour polymères - Google Patents

Préparation stabilisante pour polymères Download PDF

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Publication number
WO2007088114A1
WO2007088114A1 PCT/EP2007/050579 EP2007050579W WO2007088114A1 WO 2007088114 A1 WO2007088114 A1 WO 2007088114A1 EP 2007050579 W EP2007050579 W EP 2007050579W WO 2007088114 A1 WO2007088114 A1 WO 2007088114A1
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WIPO (PCT)
Prior art keywords
carbon atoms
alkyl
substituted
bis
phenyl
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PCT/EP2007/050579
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English (en)
Inventor
Cesare Lorenzetti
Michela Bonora
Anna Bassi
Mirko Rossi
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Ciba Holding Inc.
Ciba S.P.A.
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Priority to CA2636831A priority Critical patent/CA2636831C/fr
Priority to ES07704047T priority patent/ES2398248T3/es
Priority to EP07704047A priority patent/EP1979406B1/fr
Priority to JP2008552776A priority patent/JP5308165B2/ja
Priority to KR1020087018679A priority patent/KR101368176B1/ko
Priority to CN2007800041832A priority patent/CN101379122B/zh
Application filed by Ciba Holding Inc., Ciba S.P.A. filed Critical Ciba Holding Inc.
Priority to BRPI0707359A priority patent/BRPI0707359B1/pt
Priority to US12/223,141 priority patent/US8173728B2/en
Priority to PL07704047T priority patent/PL1979406T3/pl
Publication of WO2007088114A1 publication Critical patent/WO2007088114A1/fr
Priority to IL192789A priority patent/IL192789A0/en
Priority to EC2008008659A priority patent/ECSP088659A/es

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
    • C08K5/005—Stabilisers against oxidation, heat, light, ozone
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/17—Amines; Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3432—Six-membered rings
    • C08K5/3435—Piperidines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
    • C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L23/04—Homopolymers or copolymers of ethene
    • C08L23/06—Polyethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/20—Carboxylic acid amides
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3467—Heterocyclic compounds having nitrogen in the ring having more than two nitrogen atoms in the ring
    • C08K5/3477—Six-membered rings
    • C08K5/3492—Triazines
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L79/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen with or without oxygen or carbon only, not provided for in groups C08L61/00 - C08L77/00
    • C08L79/02—Polyamines

Definitions

  • the invention relates to stabilized thermoplastic polymers, in particular polyolefin films.
  • the stabilizing composition contains a tertiary amine with a molecular weight greater than 400 g/mol, a UV-absorber and/or a sterically hindered amine light stabilizer (HALS). Further aspects of the invention are a process for stabilizing thermoplastic polymers and the use of the above composition for stabilizing thermoplastic polymers.
  • Tertiary amines in particular bridged amine compounds, such as diazabicyclooctane (DABCO) and triazadamantane derivatives in combination with sterically hindered amines are disclosed in WO 00/09604 and in WO 98/36023.
  • DABCO diazabicyclooctane
  • the tertiary amines described therein are all of low molecular weight, which leads to problems during processing of the polymers due to their volatility and high migration rate.
  • UV-absorbers is particularly good.
  • UV-absorbers tertiary amines and HALS provides in many cases the best stabilization.
  • UV-absorbers are increased.
  • hydroxyphenyl triazine UV-absorbers are relatively susceptible to the interaction with pesticides, especially towards sulphur-based pesticides.
  • the use of a small amount of an aliphatic tertiary amine with high molecular weight increases their durability, that is, their persistency in the polymer articles.
  • LDPE low density polyethylene
  • LLDPE linear low density polyethylene
  • EVA ethylvinylacetate
  • EBA ethylene/butylacrylate
  • antioxidants such as phenols, phosphates, lactones or hydroxylamines
  • slip agents such as anti-blocking additives, such as erucamide, oleamide or silica
  • mineral fillers such as kaolin, Ca carbonate, Barium sulphate, carbon black, hydrotalcite and pigments, such as Smartlight® RL 1000. They are typically stabilized with HALS, with or without UV-absorbers.
  • Beside films, raffia, for example made of HDPE, PP, LDPE is frequently used with the same purposes in greenhouse or mulching applications.
  • the films and raffia are frequently exposed to the chemicals utilized as pesticides, herbicides and soil disinfectants used to protect crops and flowers. Very often, such compounds are based on chlorine, sulphur and metals (Cu, Fe). All these species are able to react with the stabilizers, leading to premature degradation of the film. Sulphur is known to be very effective, both as elemental powder sublimated or sprayed in the greenhouses and as part of active molecules (e.g. Vapam).
  • sulphur and sulphur-based compounds can interact with hydroxyphenil-triazines, leading not only to premature degradation but also to the loss of the UV-filter effect, used to improve productivity of the crops.
  • Some types of crops are in fact degraded by the UV-components of solar radiation, which must be filtered off to obtain high quality and yields. Additionally, some micro-organisms, e.g. Botrytis Cinerea, can proliferate under specific UV-irradiation. These pests are harmful for the cultivation of some varieties of roses [R. Reuven et al., Development of photoselective PE films for control of foliar pathogens in greenhouse-grown crops, Plasticulture No. 102, pg. 7 (1994); Y. Eheshel et al., "The use of UV absorbing plastic sheets to protect crops against insects and spread of virus diseases", CIPA Congress 1997].
  • PP or PE tapes used as artificial grass are another application that combines a high exposure to UV-light (with the subsequent need for stabilization) with contamination of sulphur, used as vulcanizer for the rubber that represents the bottom of the artificial grass.
  • the stability of such systems can be further affected by the presence of pigments that can act as pro-degradants.
  • One aspect of the invention is a stabilized polymer composition
  • a stabilized polymer composition comprising a) a thermoplastic polymer; b) a tertiary amine with a molecular weight greater than 400 g/mol, which is not a 2,2,6,6 tetramethylpiperidine derivative; c1 ) a UV-absorber selected from the group consisting of the hydroxyphenyl benzotriazoles, hydroxyphenyl triazines, hydroxy benzophenones and oxalic anilides; or c2) a light stabilizer from the class of sterically hindered amines; or c3) a mixture of the UV-absorber, component c1 ) and the sterically hindered amine, component c2).
  • one aspect of the invention is a stabilized polymer composition
  • a stabilized polymer composition comprising a) a non halogen containing thermoplastic polymer; b) an aliphatic tertiary amine with a molecular weight greater than 400 g/mol, which is not a 2,2,6,6 tetramethylpiperidine derivative; c1 ) a UV-absorber selected from the group consisting of the hydroxyphenyl benzotriazoles, hydroxyphenyl triazines, hydroxy benzophenones and oxalic anilides; or c2) a light stabilizer from the class of sterically hindered amines; or c3) a mixture of the UV-absorber, component c1 ) and the sterically hindered amine, component c2).
  • the tertiary amine has a molecular weight of more than 500 g/mol, in particular of more than 700 g/mol.
  • the composition comprises a tertiary amine and a UV- absorber, as defined above.
  • the composition comprises a tertiary amine, a UV-absorber and a sterically hindered amine.
  • thermoplastic polymers examples are given below.
  • Polymers of monoolefins and diolefins for example polypropylene, polyisobutylene, po- lybut-1-ene, poly-4-methylpent-1-ene, polyvinylcyclohexane, polyisoprene or polybutadiene, as well as polymers of cycloolefins, for instance of cyclopentene or norbornene, polyethylene (which optionally can be crosslinked), for example high density polyethylene (HDPE), high density and high molecular weight polyethylene (HDPE-HMW), high density and ultrahigh molecular weight polyethylene (HDPE-UHMW), medium density polyethylene (MDPE), low density polyethylene (LDPE), linear low density polyethylene (LLDPE), (VLDPE) and (ULDPE).
  • HDPE high density polyethylene
  • HDPE-HMW high density and high molecular weight polyethylene
  • HDPE-UHMW high density and ultrahigh molecular weight polyethylene
  • MDPE medium density polyethylene
  • Polyolefins i.e. the polymers of monoolefins exemplified in the preceding paragraph, preferably polyethylene and polypropylene, can be prepared by different, and especially by the following, methods:
  • a catalyst that normally contains one or more than one metal of groups IVb, Vb, VIb or VIII of the Periodic Table.
  • These metals usually have one or more than one ligand, typically oxides, halides, alcoholates, esters, ethers, amines, alkyls, alkenyls and/or aryls that may be either ⁇ - or ⁇ -coordinated.
  • These metal complexes may be in the free form or fixed on substrates, typically on activated magnesium chloride, titanium(lll) chloride, alumina or silicon oxide.
  • These catalysts may be soluble or insoluble in the polymerisation medium.
  • the catalysts can be used by themselves in the polymerisation or further activators may be used, typically metal alkyls, metal hydrides, metal alkyl halides, metal alkyl oxides or metal alkyloxanes, said metals being elements of groups Ia, Ma and/or MIa of the Periodic
  • the activators may be modified conveniently with further ester, ether, amine or silyl ether groups. These catalyst systems are usually termed Phillips, Standard Oil Indiana, Ziegler (-Natta), TNZ (DuPont), metallocene or single site catalysts (SSC).
  • Mixtures of the polymers mentioned under 1 for example mixtures of polypropylene with polyisobutylene, polypropylene with polyethylene (for example PP/HDPE, PP/LDPE) and mixtures of different types of polyethylene (for example LDPE/HDPE).
  • Copolymers of monoolefins and diolefins with each other or with other vinyl monomers for example ethylene/propylene copolymers, linear low density polyethylene (LLDPE) and mixtures thereof with low density polyethylene (LDPE), propylene/but-1-ene copolymers, propylene/isobutylene copolymers, ethylene/but-1-ene copolymers, ethylene/hexene copolymers, ethylene/methylpentene copolymers, ethylene/heptene copolymers, ethylene/octene copolymers, ethylene/vinylcyclohexane copolymers, ethylene/cycloolefin copolymers (e.g.
  • ethylene/norbornene like COC ethylene/1 -olefins copolymers, where the 1 -olefin is generated in-situ; propylene/butadiene copolymers, isobutylene/isoprene copolymers, ethylene/vi- nylcyclohexene copolymers, ethylene/alkyl acrylate copolymers, ethylene/alkyl methacrylate copolymers, ethylene/vinyl acetate copolymers or ethylene/acrylic acid copolymers and their salts (ionomers) as well as terpolymers of ethylene with propylene and a diene such as hexadiene, dicyclopentadiene or ethylidene-norbornene; and mixtures of such copolymers with one another and with polymers mentioned in 1 ) above, for example polypropylene/ethy- lene-propylene copolymers, LD
  • Hydrocarbon resins for example C 5 -C 9
  • hydrogenated modifications thereof e.g. tackifiers
  • mixtures of polyalkylenes and starch
  • Homopolymers and copolymers from 1.) - 4.) may have any stereostructure including syndio- tactic, isotactic, hemi-isotactic or atactic; where atactic polymers are preferred. Stereoblock polymers are also included.
  • Polystyrene poly(p-methylstyrene), poly( ⁇ -methylstyrene).
  • Homopolymers and copolymers may have any stereostructure including syndiotactic, isotactic, hemi-isotactic or atactic; where atactic polymers are preferred. Stereoblock polymers are also included.
  • Copolymers including aforementioned vinyl aromatic monomers and comonomers selected from ethylene, propylene, dienes, nitriles, acids, maleic anhydrides, maleimides, vinyl acetate and vinyl chloride or acrylic derivatives and mixtures thereof, for example styrene/bu- tadiene, styrene/acrylonitrile, styrene/ethylene (interpolymers), styrene/alkyl methacrylate, styrene/butadiene/alkyl acrylate, styrene/butadiene/alkyl methacrylate, styrene/maleic anhy- dride, styrene/acrylonitrile/methyl acrylate; mixtures of high impact strength of styrene copolymers and another polymer, for example a polyacrylate, a diene polymer or an ethylene/pro- pylene/diene terpoly
  • Hydrogenated aromatic polymers derived from hydrogenation of polymers mentioned under 6. especially including polycyclohexylethylene (PCHE) prepared by hydrogenating atactic polystyrene, often referred to as polyvinylcyclohexane (PVCH).
  • PCHE polycyclohexylethylene
  • PVCH polyvinylcyclohexane
  • Homopolymers and copolymers may have any stereostructure including syndiotactic, isotac- tic, hemi-isotactic or atactic; where atactic polymers are preferred.
  • Stereoblock polymers are also included.
  • Graft copolymers of vinyl aromatic monomers such as styrene or ⁇ -methylstyrene, for example styrene on polybutadiene, styrene on polybutadiene-styrene or polybutadiene-acry- lonitrile copolymers; styrene and acrylonitrile (or methacrylonitrile) on polybutadiene; styrene, acrylonitrile and methyl methacrylate on polybutadiene; styrene and maleic anhydride on polybutadiene; styrene, acrylonitrile and maleic anhydride or maleimide on polybutadiene; styrene and maleimide on polybutadiene; styrene and alkyl acrylates or methacrylates on polybutadiene; styrene and acrylonitrile on ethylene/propylene/diene terpoly
  • Polymers derived from ⁇ , ⁇ -unsatu rated acids and derivatives thereof such as polyacry- lates and polymethacrylates; polymethyl methacrylates, polyacrylamides and polyacryloni- triles, impact-modified with butyl acrylate.
  • Copolymers of the monomers mentioned under 8) with each other or with other unsaturated monomers for example acrylonitrile/ butadiene copolymers, acrylonitrile/alkyl acrylate copolymers, acrylonitrile/alkoxyalkyl acrylate or acrylonitrile/vinyl halide copolymers or acry- lonitrile/ alkyl methacrylate/butadiene terpolymers.
  • Polymers derived from unsaturated alcohols and amines or the acyl derivatives or ace- tals thereof for example polyvinyl alcohol, polyvinyl acetate, polyvinyl stearate, polyvinyl benzoate, polyvinyl maleate, polyvinyl butyral, polyallyl phthalate or polyallyl melamine; as well as their copolymers with olefins mentioned in 1 ) above.
  • Polyacetals such as polyoxymethylene and those polyoxymethylenes which contain ethylene oxide as a comonomer; polyacetals modified with thermoplastic polyurethanes, acrylates or MBS.
  • Polyamides and copolyamides derived from diamines and dicarboxylic acids and/or from aminocarboxylic acids or the corresponding lactams for example polyamide 4, polyamide 6, polyamide 6/6, 6/10, 6/9, 6/12, 4/6, 12/12, polyamide 1 1 , polyamide 12, aromatic polyamides starting from m-xylene diamine and adipic acid; polyamides prepared from hexamethylenediamine and isophthalic or/and terephthalic acid and with or without an elastomer as modifier, for example poly-2,4,4,-trimethylhexamethylene terephthalamide or poly- m-phenylene isophthalamide; and also block copolymers of the aforementioned polyamides with polyolefins, olefin copolymers, ionomers or chemically bonded or grafted elastomers; or with polyethers, e.g.
  • polyethylene glycol polypropylene glycol or polytetramethylene glycol
  • polyamides or copolyamides modified with EPDM or ABS polyamides condensed during processing
  • RIM polyamide systems polyamides condensed during processing
  • Polyureas polyimides, polyamide-imides, polyetherimids, polyesterimids, polyhydantoins and polybenzimidazoles.
  • Polyesters derived from dicarboxylic acids and diols and/or from hydroxycarboxylic acids or the corresponding lactones for example polyethylene terephthalate, polybutylene tereph- thalate, poly-M-dimethylolcyclohexane terephthalate, polyalkylene naphthalate (PAN) and polyhydroxybenzoates, as well as block copolyether esters derived from hydroxyl-terminated polyethers; and also polyesters modified with polycarbonates or MBS.
  • Blends of the aforementioned polymers for example PP/EPDM, PoIy- amide/EPDM or ABS, PVC/EVA, PVC/ABS, PVC/MBS, PC/ABS, PBTP/ABS, PC/ASA, PC/PBT, PVC/CPE, PVC/acrylates, POM/thermoplastic PUR, PC/thermoplastic PUR, POM/acrylate, POM/MBS, PPO/HIPS, PPO/PA 6.6 and copolymers, PA/HDPE, PA/PP, PA/PPO, PBT/PC/ABS or PBT/PET/PC.
  • polyblends for example PP/EPDM, PoIy- amide/EPDM or ABS, PVC/EVA, PVC/ABS, PVC/MBS, PC/ABS, PBTP/ABS, PC/ASA, PC/PBT, PVC/CPE, PVC/acrylates, POM/thermoplastic PUR, PC/thermoplastic PUR, POM/
  • thermoplastic polymer is low density polyethylene (LDPE), linear low density polyethylene (LLDPE), polypropylene (PP) or ethylvinylacetate (EVA).
  • LDPE low density polyethylene
  • LLDPE linear low density polyethylene
  • PP polypropylene
  • EVA ethylvinylacetate
  • composition in the form of a film or tape.
  • hydroxybenzophenone is of formula I
  • the 2-hydroxyphenylbenzotriazole is of formula Na, Mb or Nc
  • v is an integer from 1 to 3 and w is 1 or 2 and the substituents Z independently of one another are hydrogen, halogen, hydroxyl or alkoxy having 1 to 12 carbon atoms;
  • Ri is hydrogen, alkyl having 1 to 24 carbon atoms, phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety, cycloalkyl having 5 to 8 carbon atoms or a radical of the formula
  • R 4 and R 5 independently of one another are alkyl having in each case 1 to 5 carbon atoms, or R 4 , together with the radical C n H 2n +i- m , forms a cycloalkyl radical having 5 to 12 carbon atoms, m is 1 or 2, n is an integer from 2 to 20 and
  • M is a radical of the formula -COOR 6 in which
  • R 6 is hydrogen, alkyl having 1 to 12 carbon atoms, alkoxyalkyl having in each case 1 to 20 carbon atoms in the alkyl moiety and in the alkoxy moiety or phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety
  • R 2 is hydrogen, halogen, alkyl having 1 to 18 carbon atoms, and phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety
  • R 3 is hydrogen, chlorine, alkyl or alkoxy having in each case 1 to 4 carbon atoms or -COOR 6 in which R 6 is as defined above, at least one of the radicals Ri and R 2 being other than hydrogen;
  • T is hydrogen or alkyl having 1 to 6 carbon atoms
  • T 1 is hydrogen, chlorine or alkyl or alkoxy having in each case 1 to 4 carbon atoms, n is 1 or 2 and, if n is 1 ,
  • T 2 is chlorine or a radical of the formula -OT 3 or — N and,
  • T 2 is a radical of the formula or -0-Tg-O-; in which T 3 is hydrogen, alkyl which has 1 to 18 carbon atoms and is unsubstituted or substituted by 1 to 3 hydroxyl groups or by -OCOT 6 , alkyl which has 3 to 18 carbon atoms, is interrupted once or several times by -O- or -NT 6 - and is unsubstituted or substituted by hydroxyl or -OCOT 6 , cycloalkyl which has 5 to 12 carbon atoms and is unsubstituted or substituted by hydroxyl and/or alkyl having 1 to 4 carbon atoms, alkenyl which has 2 to 18 carbon atoms and is unsubstituted or substituted by hydroxyl, phenylalkyl having 1 to 4 carbon atoms in the alkyl
  • T 4 and T 5 independently of one another are hydrogen, alkyl having 1 to 18 carbon atoms, alkyl which has 3 to 18 carbon atoms and is interrupted once or several times by -O- or -NT 6 -, cycloalkyl having 5 to 12 carbon atoms, phenyl, phenyl which is substituted by alkyl having 1 to 4 carbon atoms, alkenyl having 3 to 8 carbon atoms, phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety or hydroxyalkyl having 2 to 4 carbon atoms
  • T 6 is hydrogen, alkyl having 1 to 18 carbon atoms, cycloalkyl having 5 to 12 carbon atoms, alkenyl having 3 to 8 carbon atoms, phenyl, phenyl which is substituted by alkyl having 1 to 4 carbon atoms, phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety,
  • T 7 is hydrogen, alkyl having 1 to 18 carbon atoms, phenyl which is unsubstituted or substituted by hydroxyl, phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety, or -
  • T 8 is alkyl having 1 to 18 carbon atoms, alkenyl having 3 to 8 carbon atoms, cycloalkyl having 5 to 10 carbon atoms, phenyl, phenyl which is substituted by alkyl having 1 to 4 carbon atoms, or phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety,
  • Tg is alkylene having 2 to 8 carbon atoms, alkenylene having 4 to 8 carbon atoms, alkynylene having 4 carbon atoms, cyclohexylene, alkylene which has 2 to 8 carbon atoms and is interrupted once or several times by -0-, or a radical of the formula - CH 2 CH(OH)CH 2 OT 11 OCH 2 CH(OH)CH 2 - or -CH 2 -C(CH 2 OH) 2 -CH 2 -,
  • T 10 is alkylene which has 2 to 20 carbon atoms and can be interrupted once or several times by -0-, or cyclohexylene,
  • T 11 is alkylene having 2 to 8 carbon atoms, alkylene which has 2 to 18 carbon atoms and is interrupted once or several times by -0-, 1 ,3-cyclohexylene, 1 ,4-cyclohexylene, 1 ,3- phenylene or 1 ,4-phenylene, or
  • T 10 and T 6 together with the two nitrogen atoms, are a piperazine ring; in the compounds of formula (lie)
  • R' 2 is CrCi 2 alkyl and k is a number from 1 to 4;
  • u is 1 or 2 and r is an integer from 1 to 3, the substituents
  • Yi independently of one another are hydrogen, hydroxyl, phenyl or halogen, halogenomethyl, alkyl having 1 to 12 carbon atoms, alkoxy having 1 to 18 carbon atoms, alkoxy having 1 to 18 carbon atoms which is substituted by a group -COO(CrCi 8 alkyl); if u is 1 , Y 2 is alkyl having 1 to 18 carbon atoms, phenyl which is unsubstituted or substituted by hydroxyl, halogen, alkyl or alkoxy having 1 to 18 carbon atoms; alkyl which has 1 to 12 carbon atoms and is substituted by -COOH, -COOY 8 , -CONH 2 , - CONHY 9 , -CONY 9 Y 10 , -NH 2 , -NHY 9 , -NY 9 Y 10 , -NHCOY 11 , -CN and/or -OCOY 11 ; alkyl which has 4 to 20
  • Y 2 is alkylene having 2 to 16 carbon atoms, alkenylene having 4 to 12 carbon atoms, xylylene, alkylene which has 3 to 20 carbon atoms, is interrupted by one or more -O- atoms and/or is substituted by hydroxyl, -CH 2 CH(OH)CH 2 -O-Y 15 -OCH 2 CH(OH)CH 2 , -CO-Y 16 -CO-, - CO-NH-Y 17 -NH-CO- or -(CH 2 ) m -CO 2 -Y 18 -OCO-(CH 2 ) m , in which m is 1 , 2 or 3,
  • Y 8 is alkyl having 1 to 18 carbon atoms, alkenyl having 3 to 18 carbon atoms, alkyl which has 3 to 20 carbon atoms, is interrupted by one or more oxygen or sulfur atoms or -NT 6 - and/or is substituted by hydroxyl, alkyl which has 1 to 4 carbon atoms and is substituted by - P(O)(OY 14 ) 2 , -NY 9 Y 10 or -OCOY 11 and/or hydroxyl, alkenyl having 3 to 18 carbon atoms, glycidyl, or phenylalkyl having 1 to 5 carbon atoms in the alkyl moiety,
  • Y 9 and Y 10 independently of one another are alkyl having 1 to 12 carbon atoms, alkoxyalkyl having 3 to 12 carbon atoms, dialkylaminoalkyl having 4 to 16 carbon atoms or cyclohexyl having 5 to 12 carbon atoms, or Y 9 and Y 10 together are alkylene, oxaalkylene or azaalkylene having in each case 3 to 9 carbon atoms, Y 11 is alkyl having 1 to 18 carbon atoms, alkenyl having 2 to 18 carbon atoms or phenyl,
  • Y- I2 is alkyl having 1 to 18 carbon atoms, alkenyl having 2 to 18 carbon atoms, phenyl, alkoxy having 1 to 12 carbon atoms, phenoxy, alkylamino having 1 to 12 carbon atoms or phenylamino, Yi 3 is alkyl having 1 to 18 carbon atoms, phenyl or alkylphenyl having 1 to 8 carbon atoms in the alkyl radical,
  • Y- I4 is alkyl having 1 to 12 carbon atoms or phenyl
  • Y 15 is alkylene having 2 to 10 carbon atoms, phenylene or a group -phenylene-M-phenylene- in which M is -O-, -S-, -SO 2 -, -CH 2 - or -C(CH 3 ) 2 -, Y 16 is alkylene, oxaalkylene or thiaalkylene having in each case 2 to 10 carbon atoms, phenylene or alkenylene having 2 to 6 carbon atoms,
  • Y 17 is alkylene having 2 to 10 carbon atoms, phenylene or alkylphenylene having 1 to 1 1 carbon atoms in the alkyl moiety, and
  • Y 18 is alkylene having 2 to 10 carbon atoms or alkylene which has 4 to 20 carbon atoms and is interrupted once or several times by oxygen; in the compounds of the formula (IV) x is an integer from 1 to 3 and the substituents L independently of one another are hydrogen, alkyl, alkoxy or alkylthio having in each case 1 to
  • CrCi 8 alkyl may be linear or branched.
  • alkyl having up to 18 carbon atoms are methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 2-ethylbutyl, n-pentyl, isopentyl, 1-methylpentyl, 1 ,3-dimethylbutyl, n-hexyl, 1-methylhexyl, n-heptyl, isoheptyl, 1 ,1 ,3,3-tetramethylbutyl, 1-methylheptyl, 3-methylheptyl, n-octyl, 2-ethylhexyl, 1 ,1 ,3-trimethyl- hexyl, 1 ,1 ,3,3-tetramethylpentyl, nonyl, decyl, undecyl, 1-methylundecyl,
  • Ri can be hydrogen or alkyl having 1 to 24 carbon atoms, such as methyl, ethyl, propyl, butyl, hexyl, octyl, nonyl, dodecyl, tetradecyl, hexadecyl, octadecyl, nonadecyl and eicosyl and also corresponding branched isomers.
  • R 1 can also be cycloalkyl having 5 to 8 carbon atoms, for example
  • R 4 and R 5 independently of one another are alkyl having in each case 1 to 5 carbon atoms, in particular methyl, or R 4 , together with the C n H 2n +i- m radical, forms a cycloalkyl radical having 5 to 12 carbon atoms, for example cyclohexyl, cyclooctyl and cyclodecyl.
  • M is a radical of the formula -COOR 6 in which R 6 is not only hydrogen but also alkyl having 1 to 12 carbon atoms or alkoxyalkyl having 1 to 20 carbon atoms in each of the alkyl and alkoxy moieties. Suitable alkyl radicals R 6 are those enumerated for R 1 .
  • alkoxyalkyl groups are -CaH 4 OCaH 5 , -CaH 4 OCeH 17 and -C 4 H 8 OC 4 Hg.
  • R 6 is, for example, benzyl, cumyl, ⁇ -methylbenzyl or phenylbutyl.
  • R 2 can also be alkyl having 1 to 18 carbon atoms. Examples of such alkyl radicals are indicated in the definitions of R 1 .
  • R 2 can also be phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety, for example benzyl, a-methylbenzyl and cumyl.
  • Halogen as a substituent means in all cases fluorine, chlorine, bromine or iodine, preferably chlorine or bromine and more preferably chlorine.
  • At least one of the radicals R 1 and R 2 must be other than hydrogen.
  • R 3 is also alkyl or alkoxy having in each case 1 to 4 carbon atoms, for example methyl, butyl, methoxy and ethoxy, and also -COOR 6 .
  • T is hydrogen or alkyl having 1 to 6 carbon atoms, such as methyl and butyl
  • T 1 is not only hydrogen or chlorine, but also alkyl or alkoxy having in each case 1 to 4 carbon atoms, for example methyl, methoxy and butoxy
  • T 2 is chlorine or a radical of the formula -OT 3 or -NT 4 T 5
  • T 3 is here hydrogen or alkyl having 1 to 18 carbon atoms (cf. the definition of R 1 ).
  • These alkyl radicals can be substituted by 1 to 3 hydroxyl groups or by a radical -OCOT 6 .
  • T 3 can be alkyl having 3 to 18 carbon atoms (cf.
  • R 1 which is interrupted once or several times by -O- or -NT 6 - and is unsubstituted or substituted by hydroxyl or -OCOT 6 .
  • T 3 as cycloalkyl are cyclopentyl, cyclohexyl or cyclooctyl.
  • T 3 can also be alkenyl having 2 to 18 carbon atoms. Suitable alkenyl radicals are derived from the alkyl radicals enumerated in the definitions of R 1 . These alkenyl radicals can be substituted by hydroxyl.
  • T 3 as phenylalkyl are benzyl, phenylethyl, cumyl, ⁇ -methylbenzyl or benzyl.
  • T 3 can also be a radical of the formula O
  • T 4 and T 5 can, independently of one another, be not only hydrogen but also alkyl having 1 to 18 carbon atoms or alkyl which has 3 to 18 carbon atoms and is interrupted once or several times by -O- or -NT 6 -.
  • T 4 and T 5 can also be cycloalkyl having 5 to 12 carbon atoms, for example cyclopentyl, cyclohexyl and cyclooctyl.
  • Examples of T 4 and T 5 as alkenyl groups can be found in the illustrations of T 3 .
  • Examples of T 4 and T 5 as phenylalkyl having 1 to 4 carbon atoms in the alkyl moiety are benzyl or phenylbutyl.
  • these substituents can also be hydroxyalkyl having 1 to 3 carbon atoms.
  • T 2 is a divalent radical of the formula / 10 ⁇ or -0-Tg-O-.
  • T 6 is alkyl, cycloalkyl, alkenyl, aryl or phenylalkyl; examples of such radicals have already been given above.
  • T 7 can be phenyl or hydroxyphenyl and also -CH 2 OT 8 in which T 8 can be one of the alkyl, alkenyl, cycloalkyl, aryl or phenylalkyl radicals enumerated.
  • the divalent radical Tg can be alkylene having 2 to 8 carbon atoms, and such radicals can also be branched. This also applies to the alkenylene and alkynylene radicals Tg. As well as cyclohexylene, Tg can also be a radical of the formula CH 2 CH(OH)CH 2 OT 11 OCH 2 CH(OH)CH 2 - or -CH 2 -C(CH 2 OH) 2 -CH 2 -.
  • T 10 is a divalent radical and, in addition to cyclohexylene, is also alkylene which has 2 to 20 carbon atoms and which can be interrupted once or several times by -0-.
  • Suitable alkylene radicals are derived from the alkyl radicals mentioned in the definitions of R 1 .
  • T 11 is also an alkylene radical. It contains 2 to 8 carbon atoms or, if it is interrupted once or several times by -0-, 4 to 10 carbon atoms. T 11 is also 1 ,3-cyclohexylene, 1 ,4-cyclohexylene, 1 ,3-phenylene or 1 ,4-phenylene.
  • T 6 and T 10 can also be a piperazine ring.
  • alkyl, alkoxy, phenylalkyl, alkylene, alkenylene, alkoxyalkyl and cycloalkyl radicals and also alkylthio, oxaalkylene or azoalkylene radicals in the compounds of the formulae (I), (Ma), (Mb), (Mc), (III) and IV) can be deduced from the above statements.
  • UV absorbers of the formulae (I), (Ma), (Mb), (lie), (III) and (IV) are known per se and are described, together with their preparation in, for example, WO 96/28431 , EP-A-323 408, EP- A-57 160, US 5 736 597 (EP-A-434 608), US 4 619 956, DE-A 31 35 810 and GB-A 1 336 391. Preferred meanings of substituents and individual compounds can be deduced from the documents mentioned.
  • UV-absorber of the class of hydroxyphenyl triazines is of formula (IV)
  • n 1 or 2;
  • R 1 C 2 -C 6 alkenyl; C 1 - C 12 alkoxy; C 2 -C 18 alkenoxy; halogen; trifluoromethyl; C ⁇ C ⁇ phenylalkyl; phenyl; phenyl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy or halogen; phenoxy; or phenoxy which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy or halogen;
  • R, and R. independently of one another, are H, C -C..alkyl; OR' ; C -C.alkenyl; C - C 18 alkenoxy; halogen; trifluoromethyl; C 7 -C 11 phenylalkyl; phenyl; phenyl which is substituted by C 1 -C 18 alkyl, C 1 -C 18 alkoxy or halogen; phenoxy; or phenoxy which is substituted by C 1 - C 18 alkyl, C 1 -C 18 aIkoxy or halogen; R. is hydrogen, C -C.,alkyl, C -C 12 cycloalkyl or C -C 15 phenylalkyl;
  • R 8 is C 1 -C 18 alkyl; C 2 -C 18 alkenyl; hydroxyethyl; C 3 -C 50 alkyl which is interrupted by O, NH, NR Q y or S and/or is substituted by OH; C ⁇ alkyl which is substituted by -P(O)(OR 14 ) 2 , -N(R 9 )(R 10 ) or -OCOR 11 and/or OH; glycidyl; C -C 10 cycloalkyl; phenyl; C 7 -C 14 alkylphenyl or C - C ⁇ phenylalkyl;
  • R. and R 1n independently of one another, are C -C 1o alkyl; C -C 10 alkoxyalkyl; C -
  • C 16 dialkylaminoalkyl or C 5 -C 12 cycloalkyl, or R 9 and R 10 together are C 3 -C 8 alkylene or - oxaalkylene or -azaalkylene;
  • R 1 I 1 i is Ci-C 1 io D alkyl; C -C 1 Io D alkenyl or phenyl; C -C 10 hydroxyalkyl; cyclohexyl; or is C 0 -C o ⁇ Ualkyl which is interrupted by -O- and may be substituted by OH;
  • R 12 is C j -C ⁇ alkyl; C 2 -C 18 alkenyl; phenyl; C 1 -C ⁇ aIkOXy; C 3 -C 18 alkenyloxy; C 3 -C 5Q alkoxy which is interrupted by O, NH, NR 9 or S and/or substituted by OH; cyclohexyloxy; C 7 - C 14 alkylphenoxy; C ⁇ C ⁇ phenylalkoxy; phenoxy; C ⁇ C ⁇ alkylamino; phenylamino; tolylamino or naphthylamino;
  • R 13 is C j -C ⁇ alkyl; phenyl; naphthyl or C 7 -C 14 alkylphenyl;
  • R 14 is C j -C ⁇ alkyl, methylphenyl or phenyl
  • R 0n is C -C. n alkylene; C -C ⁇ alkylene which is interrupted by O, phenylene or a -phenylene-
  • X-phenylene- group in which X is -0-, -S-, -SO 2 -, -CH 2 - or -C(CH 3 ) 2 -;
  • R 21 is C 2 -C 1Q alkylene, C 2 -C 1Q oxaalkylene, C 2 -C 1Q thiaalkylene, C 6 -C 12 arylene or C 2 -
  • R 22 is C 2 -C 1Q alkylene, phenylene, tolylene, diphenylenemethane or a CH 2 -
  • R. is C -C. n alkylene or C -C. n alkylene which is interrupted by O.
  • Halogen is in all cases fluorine, chlorine, bromine or iodine.
  • alkyl examples include methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, 2- ethylbutyl, n-pentyl, isopentyl, 1-methylpentyl, 1 ,3-dimethylbutyl, n-hexyl, 1-methylhexyl, n- heptyl, isoheptyl, 1 ,1 ,3,3-tetramethylbutyl, 1-methylheptyl, 3-methylheptyl, n-octyl, 2-ethyl- hexyl, 1 ,1 ,3-trimethylhexyl, 1 ,1 ,3,3-tetramethylpentyl, nonyl, decyl, undecyl, 1-methylundecyl, dodecyl.
  • alkoxy having up to 12 carbon atoms examples include methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, pentoxy, isopentoxy, hexoxy, heptoxy, octoxy, decyloxy, dodecyloxy.
  • alkenoxy examples are propenyloxy, butenyloxy, pentenyloxy and hexenyloxy.
  • C 5 -Ci 2 cycloalkyl examples are cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl and cyclo- dodecyl.
  • Ci-C 4 Alkyl-substituted C 5 -Ci 2 cycloalkyl is for example methylcyclohexyl or dimethyl- cyclohexyl.
  • OH- and/or d-Cioalkyl-substituted phenyl is for example methylphenyl, dimethylphenyl, trimethylphenyl, tert-butylphenyl or 3,5-di-tert-butyl-4-hydroxyphenyl.
  • Alkoxy-substituted phenyl is for example methoxyphenyl dimethoxyphenyl or trimethoxy- phenyl.
  • C 7 -Cgphenylalkyl examples are benzyl and phenylethyl.
  • Cy-CgPhenylalkyl which is substituted on the phenyl radical by -OH and/or by alkyl having up to 10 carbon atoms is for example methylbenzyl, dimethylbenzyl, trimethylbenzyl, tert- butylbenzyl or 3,5-di-tert-butyl-4-hydroxybenzyl.
  • alkenyl examples are allyl, 2-methallyl, butenyl, pentenyl and hexenyl.
  • AIIyI is preferred.
  • the carbon atom in position 1 is preferably saturated.
  • alkylene examples include methylene, ethylene, propylene, trimethylene, tetramethylene, pentamethylene, 2,2-dimethyltrimethylene, hexamethylene, trimethylhexamethylene, octa- methylene and decamethylene.
  • Example s of alkenylene are butenylene, pentenylene and hexenylene.
  • C 6 -Ci 2 arylene is preferably phenylene.
  • Alkyl interrupted by O is for example -CH 2 -CH 2 -O-CH 2 -CH 3 , -CH 2 -CH 2 -O-CH 3 - or -CH 2 -CH 2 - 0-CH 2 -CH 2 -CH 2 -O-CH 2 -CH 3 -. It is preferably derived from polyethlene glycol.
  • a general description is -((CH 2 ) a -O) t ,-H/CH 3 , wherein a is a number from 1 to 6 and b is a number from 2 to 10.
  • C 2 -Ci 0 oxaalkylene and C 2 -Ci 0 thiaalkylene can be deduced from the above mentioned alkylene groups by substituting one or more carbon atoms by an oxygen atom or a sulphur atom.
  • the hydroxyphenyl triazine UV-absorbers are 2-(2-hydroxyphenyl)-1 ,3,5- triazines are for example 2,4,6-tris(2-hydroxy-4-octyloxyphenyl)-1 ,3,5-triazine, 2-(2-hydroxy- 4-octyloxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1 ,3,5-triazine, 2-(2,4-dihydroxyphenyl)-4,6- bis(2,4-dimethylphenyl)-1 ,3,5-triazine, 2,4-bis(2-hydroxy-4-propyloxyphenyl)-6-(2,4- dimethylphenyl)-1 ,3,5-triazine, 2-(2-hydroxy-4-octyloxyphenyl)-4,6-bis(4-methylphenyl)-1 ,3,5- triazine, 2-(2-hydroxy-4-dodecyloxyphenyl)-4,6-
  • UV-absorbers are, for example, those according to following formulae:
  • hydroxyphenyl triazine UV-absorbers are known and partially items of commerce. They are for example disclosed in WO 96/28431.
  • 2-hydroxybenzophenones are for example the 4-hydroxy, 4-methoxy, 4- octyloxy, 4-decyloxy, 4-dodecyloxy, 4-benzyloxy and 2'-hydroxy-4,4'-dimethoxy derivatives.
  • 2-(2'-hydroxyphenyl)benzotriazoles are for example 2-(2'-hydroxy-5'- methylphenyl)-benzotriazole, 2-(3',5'-di-tert-butyl-2'-hydroxyphenyl)benzotriazole, 2-(5'-tert- butyl-2'-hydroxyphenyl)benzotriazole, 2-(2'-hydroxy-5'-(1 ,1 ,3,3-tetramethylbutyl)phenyl)ben- zotriazole, 2-(3',5'-di-tert-butyl-2'-hydroxyphenyl)-5-chloro-benzotriazole, 2-(3'-tert-butyl- 2'- hydroxy-5'-methylphenyl)-5-chloro-benzotriazole, 2-(3'-sec-butyl-5'-tert-butyl-2'-hydroxyphe- nyl)benzotriazole, 2-(2'-sec
  • oxamides are for example 4,4'-dioctyloxyoxanilide, 2,2'- diethoxyoxanilide, 2,2'-dioctyloxy-5,5'-di-tert-butoxanilide, 2,2'-didodecyloxy-5,5'-di-tert- butoxanilide, 2-ethoxy-2'-ethyloxanilide, N,N'-bis(3-dimethylaminopropyl)oxamide, 2-ethoxy- 5-tert-butyl-2'-ethoxanilide and its mixture with 2-ethoxy-2'-ethyl-5,4'-di-tert-butoxanilide, mixtures of o- and p-methoxy-disubstituted oxanilides and mixtures of o- and p-ethoxy- disubstituted oxanilides.
  • UV-absorbers are largely items of commerce and for example known as Tinuvin® 109, 171 , 326, 327, 328, 350, 360, 384, 400, 405, 41 1 or Chimassorb® 81 from Ciba Specialty Chemicals or Cyasorb® 1 164 from Cytech Inc.
  • UV-absorbers from different classes, such as for example a benzophenone UV-absorber with a benzotriazole UV- absorber or a hydroxyphenyltriazine UV-absorber with a benzotriazole UV-absorber. If such a combination is used, the weight ratio between both UV-absorbers is for example from 1 :5 to 5:1 , for instance from 1 :3 to 3:1 , particularly 1 :1.5 to 1.5:1.
  • the sterically hindered amines are selected from the group consisting of bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, bis(2,2,6,6-tetramethyl-4-piperidyl)succinate, bis(1 ,2,2,6,6-pentamethyl-4-piperidyl)sebacate, bis(1 -octyloxy-2,2,6,6-tetramethyl-4- piperidyl)sebacate, bis(1 ,2,2,6,6-pentamethyl-4-piperidyl) n-butyl-3,5-di-tert-butyl-4- hydroxybenzylmalonate, the condensate of 1-(2-hydroxyethyl)-2,2,6,6-tetramethyl-4- hydroxypiperidine and succinic acid, linear or cyclic condensates of N,N'-bis(2,2,6,6- tetramethyl-4-piperidyl)hexamethylenediamine and
  • N-(2,2,6,6-tetramethyl-4-piperidyl)-n-dodecylsuccinimide N-(1 ,2,2,6,6- pentamethyM-piperidyO-n-dodecylsuccinimide, 2-undecyl-7,7,9,9-tetramethyl-1 -oxa-3,8-di- aza-4-oxo-spiro[4,5]decane, a reaction product of 7,7,9,9-tetramethyl-2-cycloundecyl-1-oxa- 3,8-diaza-4-oxospiro-[4,5]decane and epichlorohydrin, 1 ,1-bis(1 ,2,2,6, 6-pentamethyl-4- piperidyloxycarbonyl)-2-(4-methoxyphenyl)ethene, N,N'-bis-formyl-N,N'-bis(2,
  • DASTIB 845 (RTM), TINUVIN 770 (RTM), TINUVIN 765 (RTM), TINUVIN 144 (RTM), TINUVIN 123 (RTM), TINUVIN 371 (RTM), TINUVIN 11 1 (RTM), TINUVIN 783 (RTM), TINUVIN 791 (RTM), MARK LA 52 (RTM), MARK LA 57 (RTM), MARK LA 62 (RTM), MARK LA 67 (RTM), HOSTAVIN N 20 (RTM), HOSTAVIN N 24 (RTM), SANDUVOR 3050 (RTM), DIACETAM 5 (RTM), SUMISORB TM 61 (RTM), UVINUL 4049 (RTM), SANDUVOR PR 31 (RTM), GOODRITE UV 3034 (RTM), GOODRITE UV 3150 (RTM), GOODRITE UV 3159 (RTM), GOODRITE 3110 x 128 (RTM), UVINUL 4050 H (RTM), CHIMASSORB
  • TINUVIN 770 RTM
  • TINUVIN 371 RTM
  • TINUVIN 791 RTM
  • TINUVIN 622 RTM
  • TINUVIN 783 RTM
  • CHIMASSORB 944 RTM
  • CHIMASSORB 2020 RTM
  • CHIMASSORB 1 19 RTM
  • tertiary amines are compounds of formulae (a) to (j)
  • R 30 i, R30 2 and R303 are independently Ci O -C 3 6alkyl
  • R304, R305 and R306 are independently C 9 -C 3 6alkyl
  • R 310 and R 311 are independently hydrogen or d-Ci ⁇ alkyl
  • R 307 and R 30 S are independently CrC 8 alkylene; k is a number from n is a number from 2 to 20; m is a number from 4 to 20; and x, y independently are numbers from 3 to 20.
  • the tertiary amines are largely items of commerce or can be prepared according to standard methods.
  • the tertiary amine is present in an amount of 0.1-2%, preferably 0.2-1 % by weight, based on the weight of the thermoplastic polymer.
  • the UV-absorber is present in an amount of 0.01-2% preferably 0.2-2% by weight, based on the weight of the thermoplastic polymer.
  • the sterically hindered amine is present in an amount of 0.01-2%, preferably 0.1-1 % by weight, based on the weight of the thermoplastic polymer.
  • the total amount of tertiary amine, UV-absorber and/or sterically hindered amine is from 0.2 to 4% by weight based on the weight of the thermoplastic polymer.
  • the stabilized material may additionally also contain various conventional additives, for example: 1. Antioxidants
  • Alkylated monophenols for example 2,6-di-tert-butyl-4-methylphenol, 2-tert-butyl-4,6-di- methylphenol, 2,6-di-tert-butyl-4-ethylphenol, 2,6-di-tert-butyl-4-n-butylphenol, 2,6-di-tert-bu- tyl-4-isobutylphenol, 2,6-dicyclopentyl-4-methylphenol, 2-( ⁇ -methylcyclohexyl)-4,6-dimethyl- phenol, 2,6-dioctadecyl-4-methylphenol, 2,4,6-tricyclohexylphenol, 2,6-di-tert-butyl-4-meth- oxymethylphenol, nonylphenols which are linear or branched in the side chains, for example 2,6-di-nonyl-4-methylphenol, 2,4-dimethyl-6-(1 '-methylundec
  • Alkylthiomethylphenols for example 2,4-dioctylthiomethyl-6-tert-butylphenol, 2,4-dioctyl- thiomethyl-6-methylphenol, 2,4-dioctylthiomethyl-6-ethylphenol, 2,6-di-dodecylthiomethyl-4- nonylphenol.
  • Hydroquinones and alkylated hydroquinones for example 2,6-di-tert-butyl-4-methoxy- phenol, 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amylhydroquinone, 2,6-diphenyl-4-octade- cyloxyphenol, 2,6-di-tert-butylhydroquinone, 2,5-di-tert-butyl-4-hydroxyanisole, 3,5-di-tert-bu- tyl-4-hydroxyanisole, 3,5-di-tert-butyl-4-hydroxyphenyl stearate, bis(3,5-di-tert-butyl-4-hy- droxyphenyl) adipate.
  • 2,6-di-tert-butyl-4-methoxy- phenol 2,5-di-tert-butylhydroquinone, 2,5-di-tert-amyl
  • Tocopherols for example ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol, ⁇ -tocopherol and mixtures thereof (vitamin E).
  • Hydroxylated thiodiphenyl ethers for example 2,2'-thiobis(6-tert-butyl-4-methylphenol), 2,2'-thiobis(4-octylphenol), 4,4'-thiobis(6-tert-butyl-3-methylphenol), 4,4'-thiobis(6-tert-butyl-2- methylphenol), 4,4'-thiobis(3,6-di-sec-amylphenol), 4,4'-bis(2,6-dimethyl-4-hydroxyphenyl)- disulfide.
  • Alkylidenebisphenols for example 2,2'-methylenebis(6-tert-butyl-4-methylphenol), 2,2'- methylenebis(6-tert-butyl-4-ethylphenol), 2,2'-methylenebis[4-methyl-6-( ⁇ -methylcyclohexyl)- phenol], 2,2'-methylenebis(4-methyl-6-cyclohexylphenol), 2,2'-methylenebis(6-nonyl-4- methylphenol), 2,2'-methylenebis(4,6-di-tert-butylphenol), 2,2'-ethylidenebis(4,6-di-tert-butyl- phenol), 2,2'-ethylidenebis(6-tert-butyl-4-isobutylphenol), 2,2'-methylenebis[6-( ⁇ -methylben- zyl)-4-nonylphenol], 2,2'-methylenebis[6-( ⁇ , ⁇ -dimethyl
  • Hydroxybenzylated malonates for example dioctadecyl-2,2-bis(3,5-di-tert-butyl-2-hy- droxybenzyl)malonate, di-octadecyl-2-(3-tert-butyl-4-hydroxy-5-methylbenzyl)malonate, di- dodecylmercaptoethyl-2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate, bis[4-(1 ,1 ,3,3-te- tramethylbutyl)phenyl]-2,2-bis(3,5-di-tert-butyl-4-hydroxybenzyl)malonate.
  • dioctadecyl-2,2-bis(3,5-di-tert-butyl-2-hy- droxybenzyl)malonate di-octadecyl-2-(3-tert-butyl-4-
  • Aromatic hydroxybenzyl compounds for example 1 ,3,5-tris(3,5-di-tert-butyl-4-hydroxy- benzyl)-2,4,6-trimethylbenzene, 1 ,4-bis(3,5-di-tert-butyl-4-hydroxybenzyl)-2,3,5,6-tetrame- thylbenzene, 2,4,6-tris(3,5-di-tert-butyl-4-hydroxybenzyl)phenol.
  • Triazine compounds for example 2,4-bis(octylmercapto)-6-(3,5-di-tert-butyl-4-hydroxy- anilino)-1 ,3,5-triazine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyanilino)-1 ,3,5-tri- azine, 2-octylmercapto-4,6-bis(3,5-di-tert-butyl-4-hydroxyphenoxy)-1 ,3,5-triazine, 2,4,6-tris- (3,5-di-tert-butyl-4-hydroxyphenoxy)-1 ,2,3-triazine, 1 ,3,5-tris(3,5-di-tert-butyl-4-hydroxyben- zyl)isocyanurate, 1 ,3,5-tris(4-tert-butyl-3-hydroxy-2,6-dimethylbenzyl
  • Benzylphosphonat.es for example dimethyl-2,5-di-tert-butyl-4-hydroxybenzylphospho- nate, diethyl-3,5-di-tert-butyl-4-hydroxybenzylphosphonate, dioctadecyl3,5-di-tert-butyl-4-hy- droxybenzylphosphonate, dioctadecyl- ⁇ -tert-butyl ⁇ -hydroxy-S-methylbenzylphosphonate, the calcium salt of the monoethyl ester of 3,5-di-tert-butyl-4-hydroxybenzylphosphonic acid.
  • Acylaminophenols for example 4-hydroxylauranilide, 4-hydroxystearanilide, octyl N- (3,5-di-tert-butyl-4-hydroxyphenyl)carbamate.
  • esters of ⁇ -(3,5-di-tert-butyl-4-hvdroxyphenyl)propionic acid with mono- or polyhydric alcohols e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1 ,6-hexanediol, 1 ,9- nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethy- lene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hy- droxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylol- propane, 4-hydroxy
  • esters of ⁇ -(5-tert-butyl-4-hvdroxy-3-methylphenyl)propionic acid with mono- or poly- hydric alcohols e.g. with methanol, ethanol, n-octanol, i-octanol, octadecanol, 1 ,6-hexanediol, 1 ,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis- (hydroxyethyl)oxamide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethyl- olpropane, 4-hydroxymethyl-1 -
  • esters of ⁇ -O. ⁇ -dicvclohexyl ⁇ -hvdroxyphenvDpropionic acid with mono- or polyhydric alcohols e.g. with methanol, ethanol, octanol, octadecanol, 1 ,6-hexanediol, 1 ,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, tri- ethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hydroxyethyl)ox- amide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hy- droxymethyl-i-phospha ⁇ . ⁇ j-trione
  • esters of 3,5-di-tert-butyl-4-hvdroxyphenyl acetic acid with mono- or polyhydric alcohols e.g. with methanol, ethanol, octanol, octadecanol, 1 ,6-hexanediol, 1 ,9-nonanediol, ethylene glycol, 1 ,2-propanediol, neopentyl glycol, thiodiethylene glycol, diethylene glycol, triethylene glycol, pentaerythritol, tris(hydroxyethyl)isocyanurate, N,N'-bis(hydroxyethyl)ox- amide, 3-thiaundecanol, 3-thiapentadecanol, trimethylhexanediol, trimethylolpropane, 4-hy- droxymethyl-i-phospha ⁇ . ⁇ j-trioxabicyclo
  • Aminic antioxidants for example N,N'-di-isopropyl-p-phenylenediamine, N,N'-di-sec-bu- tyl-p-phenylenediamine, N,N'-bis(1 ,4-dimethylpentyl)-p-phenylenediamine, N,N'-bis(1-ethyl-3- methylpentyl)-p-phenylenediamine, N,N'-bis(1-methylheptyl)-p-phenylenediamine, N,N'-dicy- clohexyl-p-phenylenediamine, N,N'-diphenyl-p-phenylenediamine, N,N'-bis(2-naphthyl)-p- phenylenediamine, N-isopropyl-N'-phenyl-p-phenylenediamine, N-(1 ,3-dimethylbutyl
  • Metal deactivators for example N,N'-diphenyloxamide, N-salicylal-N'-salicyloyl hydrazine, N,N'-bis(salicyloyl)hydrazine, N,N'-bis(3,5-di-tert-butyl-4-hydroxyphenylpropionyl)hydrazine, 3-salicyloylamino-1 ,2,4-triazole, bis(benzylidene)oxalyl dihydrazide, oxanilide, isophthaloyl dihydrazide, sebacoyl bisphenylhydrazide, N,N'-diacetyladipoyl dihydrazide, N,N'-bis(salicyl- oyl)oxalyl dihydrazide, N,N'-bis(salicyloyl)thiopropionyl dihydrazide.
  • Phosphites and phosphonites for example triphenyl phosphite, diphenylalkyl phosphites, phenyldialkyl phosphites, tris(nonylphenyl) phosphite, trilauryl phosphite, trioctadecyl phos- phite, distearylpentaerythritol diphosphite, tris(2,4-di-tert-butylphenyl) phosphite, diisodecyl pentaerythritol diphosphite, bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite, bis(2,4-di- cumylphenyl)pentaerythritol diphosphite, bis(2,6-di-tert-butyl-4-methylphenyl)pentaerythrito
  • Tris(2,4-di-tert-butylphenyl) phosphite (lrgafos ® 168, Ciba-Geigy), tris(nonylphenyl) phosphite,
  • Hydroxylamines for example N,N-dibenzylhydroxylamine, N,N-diethylhydroxylamine, N 1 N- dioctylhydroxylamine, N.N-dilaurylhydroxylamine, N,N-ditetradecylhydroxylamine, N 1 N- dihexadecylhydroxylamine, N.N-dioctadecylhydroxylamine, N-hexadecyl-N-octadecylhydrox- ylamine, N-heptadecyl-N-octadecylhydroxylamine, N,N-dialkylhydroxylamine derived from hydrogenated tallow amine.
  • Nitrones for example N-benzyl-alpha-phenylnitrone, N-ethyl-alpha-methylnitrone, N-octyl- alpha-heptylnitrone, N-lauryl-alpha-undecylnitrone, N-tetradecyl-alpha-tridecylnitrone, N- hexadecyl-alpha-pentadecylnitrone, N-octadecyl-alpha-heptadecylnitrone, N-hexadecyl-al- pha-heptadecylnitrone, N-ocatadecyl-alpha-pentadecylnitrone, N-heptadecyl-alpha-hepta- decylnitrone, N-octadecyl-alpha-hexadecylnitrone, nitrone derived from N,N
  • Thiosynergists for example dilauryl thiodipropionate or distearyl thiodipropionate.
  • Peroxide scavengers for example esters of ⁇ -thiodipropionic acid, for example the lauryl, stearyl, myristyl or tridecyl esters, mercaptobenzimidazole or the zinc salt of 2-mercapto- benzimidazole, zinc dibutyldithiocarbamate, dioctadecyl disulfide, pentaerythritol tetrakis( ⁇ - dodecylmercapto)propionate.
  • esters of ⁇ -thiodipropionic acid for example the lauryl, stearyl, myristyl or tridecyl esters
  • mercaptobenzimidazole or the zinc salt of 2-mercapto- benzimidazole zinc dibutyldithiocarbamate
  • dioctadecyl disulfide pentaerythritol tetrakis( ⁇ - dodecyl
  • Basic co-stabilisers for example melamine, polyvinylpyrrolidone, dicyandiamide, triallyl cyanurate, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes, alkali metal salts and alkaline earth metal salts of higher fatty acids, for example calcium stearate, zinc stearate, magnesium behenate, magnesium stearate, sodium ricinoleate and potassium palmitate, antimony pyrocatecholate or zinc pyrocatecholate. 9.
  • Nucleating agents for example inorganic substances, such as talcum, metal oxides, such as titanium dioxide or magnesium oxide, phosphates, carbonates or sulfates of, preferably, alkaline earth metals; organic compounds, such as mono- or polycarboxylic acids and the salts thereof, e.g. 4-tert-butylbenzoic acid, adipic acid, diphenylacetic acid, sodium succinate or sodium benzoate; polymeric compounds, such as ionic copolymers (ionomers).
  • inorganic substances such as talcum, metal oxides, such as titanium dioxide or magnesium oxide, phosphates, carbonates or sulfates of, preferably, alkaline earth metals
  • organic compounds such as mono- or polycarboxylic acids and the salts thereof, e.g. 4-tert-butylbenzoic acid, adipic acid, diphenylacetic acid, sodium succinate or sodium benzoate
  • polymeric compounds such as ionic copolymers (
  • Fillers and reinforcing agents for example calcium carbonate, silicates, glass fibres, glass bulbs, asbestos, talc, kaolin, mica, barium sulfate, metal oxides and hydroxides, carbon black, graphite, wood flour and flours or fibers of other natural products, synthetic fibers.
  • additives for example plasticisers, lubricants, emulsifiers, pigments, rheology additives, catalysts, flow-control agents, optical brighteners, flameproofing agents, antistatic agents and blowing agents.
  • the above mentioned further stabilizers and additives are usually applied in an amount from 0.01 % to 2%.
  • thermoplastic polymer contains additionally a further stabilizer selected from the group consisting of a phenolic antioxidant, a phosphite or phosphonite and a benzofuranone or indolinone.
  • a further stabilizer selected from the group consisting of a phenolic antioxidant, a phosphite or phosphonite and a benzofuranone or indolinone.
  • the above mentioned components and further additives can be incorporated into the thermoplastic polymer to be stabilized by known methods, for example before or during shaping or by applying the dissolved or dispersed compounds to the thermoplastic polymer, if necessary with subsequent evaporation of the solvent.
  • the components can be added to the thermoplastic polymer in the form of a powder, granules or a masterbatch, which contains these components in, for example, a concentration of from 2.5 to 25% by weight.
  • the components can be melt blended with each other before incorporation in the thermoplastic polymer. They can also be added to the thermoplastic polymer before or during the polymerization.
  • the materials stabilized according to this invention can be used in a wide variety of forms, for example as films, fibres, tapes, moulding compositions or profiles.
  • thermoplastic polymer according to the present invention examples of processing or transformation of the thermoplastic polymer according to the present invention are:
  • back injection back injection
  • slush molding injection molding, co-injection molding, forming, compression
  • compositions are preferably in the form of films useful for packaging, dump, laminating, agriculture and horticulture, greenhouse, mulch, tunnel, silage, bale wrap, swimming pools, waste bags, wallpaper, stretch film, raffia, desalination film, batteries, and connectors.
  • thermoplastic polymer incorporating into the thermoplastic polymer an aliphatic tertiary amine with a molecular weight greater than 400 g/mol, which is not a 2,2,6,6 tetramethylpiperidine derivative; a UV-absorber selected from the group consisting of the hydroxyphenyl benzotriazoles, hydroxyphenyl triazines, hydroxy benzophenones and oxalic anilides; or a light stabilizer from the class of sterically hindered amines; or a a mixture of the UV-absorber and the sterically hindered amine; and the use of an aliphatic tertiary amine with a molecular weight greater than 400 g/mol, which is not a 2,2,6,6
  • Polyethylenimines which have secondary and tertiary amine groups, are also suitable in the sense of the instant invention. Examples for such polyethylenimines are given below.
  • LDPE Low Density Polyethylene
  • the films were washed with water in order to remove the sulphur.
  • the degradation of UV absorber was monitored by UV-visible spectroscopy and calculated from the transmittance in the region 280-380 nm.
  • the polymer matrix degradation was followed by carbonyl increment using FT-IR spectroscopy.
  • Table 1 shows the carbonyl increment and surprisingly the formulations 2 and 3 look very similar although 2 does not contain HALS.
  • Table 2 residue transmittance %(280-380 nm) after WOM exposure of sulphur treated films Sample Additive content 0 hours 217 hours 462 hours 770 hours 1090 hours 0.2 % UVA 1 comparative 6 ⁇ 83 33.54 37 .26 31 .33 27 .67
  • Table 2 shows the transmittance in the range 280-380 nm of films treated with sulphur and exposed in WOM. As can be seen the transmittance of tridodecylamine containing remains low for longer time due to less degradation of the UV absorber.
  • Tables 3 and 4 respectively show the carbonyl increment and the residue elongation of films exposed in Q-UV without the sulphur contamination. As can be clearly seen the combination of tridodecylamine (TDA) and UVA 1 is able to give certain stabilization to the films also in absence of sulphur.
  • TDA tridodecylamine
  • Table 1 carbonyl increment after WOM exposure of sulphur coated films.
  • LDPE films are prepared according to example B1 , the amine used is a branched polyethylenimine (PEI) (Mw: 15000), a polymeric structure bearing both secondary and tertiary amines. Table 1 below shows the time until 50% of retained tensile elongation are reached (T50). The samples are treated with sulphur and exposed to WOM.
  • PEI polyethylenimine
  • LDPE films were prepared according to example B1 , the used amines are commercial products of Akzo Nobel (Table 1 ). Table 2 below shows the time until 50% of retained tensile elongation are reached (T50). The samples are treated with sulphur and exposed to WOM. Table 1 : Tested Amines
  • TDA tridodecylamine UVA 1 is
  • HALS 1 is Tinvuin® NOR 371 , which is described in US 6 117 995.
  • Tinuvin® 327 is a commercial UV Absorber from Ciba Specialty Chemicals.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)

Abstract

La présente invention concerne des polymères thermoplastiques stabilisés, en particulier des films polyoléfiniques. La préparation stabilisante contient une amine tertiaire de masse moléculaire supérieure à 400 g/mol, un agent absorbant d'UV et/ou un agent photostabilisant de type amine encombrée (HALS). D'autres aspects de l'invention concernent un procédé de stabilisation de polymères thermoplastiques et l'emploi de la préparation ci-avant dans la stabilisation de polymères thermoplastiques.
PCT/EP2007/050579 2006-02-01 2007-01-22 Préparation stabilisante pour polymères WO2007088114A1 (fr)

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ES07704047T ES2398248T3 (es) 2006-02-01 2007-01-22 Composición estabilizadora para polímeros
EP07704047A EP1979406B1 (fr) 2006-02-01 2007-01-22 Préparation stabilisante pour polymères
JP2008552776A JP5308165B2 (ja) 2006-02-01 2007-01-22 ポリマーのための安定剤組成物
KR1020087018679A KR101368176B1 (ko) 2006-02-01 2007-01-22 중합체용 안정화제 조성물
CN2007800041832A CN101379122B (zh) 2006-02-01 2007-01-22 用于聚合物的稳定剂组合物
CA2636831A CA2636831C (fr) 2006-02-01 2007-01-22 Preparation stabilisante pour polymeres
BRPI0707359A BRPI0707359B1 (pt) 2006-02-01 2007-01-22 composição estabilizante para polímeros
US12/223,141 US8173728B2 (en) 2006-02-01 2007-01-22 Stabilizer composition for polymers
PL07704047T PL1979406T3 (pl) 2006-02-01 2007-01-22 Kompozycja stabilizatora dla polimerów
IL192789A IL192789A0 (en) 2006-02-01 2008-07-13 Stabilizer composition for polymers
EC2008008659A ECSP088659A (es) 2006-02-01 2008-08-01 Composición estabilizante para polímeros

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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009071475A1 (fr) * 2007-12-03 2009-06-11 Basf Se Forme cristalline du 2-(4,6-bis-biphényl-4-yl-1,3,5-triazin-2-yl)-5-(2-éthyl-(n)-hexyloxy)phénol
WO2009135813A1 (fr) * 2008-05-07 2009-11-12 Basf Se Matériau dégradable
WO2010101732A1 (fr) * 2009-03-02 2010-09-10 Saudi Arabian Oil Company Stabilité améliorée vis-à-vis du rayonnement ultraviolet (uv) et durée de service améliorée de films tissés de bandes de polypropylène (pp) pour la production de gros sacs
CN101864109A (zh) * 2010-06-02 2010-10-20 王锦江 一种bopp薄膜用的复合型爽滑母料及其生产工艺
WO2011020762A1 (fr) 2009-08-18 2011-02-24 Basf Se Module photovoltaïque uv-stabilisé
US20110237715A1 (en) * 2010-03-25 2011-09-29 Basf Se Flame retardant compositions of phosphinic acid salts and nitroxyl derivatives
EP2647664A1 (fr) 2012-04-04 2013-10-09 Cytec Technology Corp. Procédé de stabilisation de films polyoléfiniques contre la dégradation par UV
EP2634296B1 (fr) 2010-10-29 2015-12-02 Dow Global Technologies LLC Bandes orientés, à base de polyéthylène et procédé de préparation associé
US9543521B2 (en) 2011-11-15 2017-01-10 Basf Se Organic semiconductor device and process for its production
CN109467903A (zh) * 2018-10-30 2019-03-15 惠州市中海源新材料科技有限公司 一种充电桩用聚碳酸酯组合物

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2009112425A1 (fr) * 2008-03-12 2009-09-17 Basf Se Film optique pour écran plat
JP5209053B2 (ja) * 2008-07-10 2013-06-12 株式会社Ａｄｅｋａ 光学フィルム
CN102834445A (zh) * 2010-03-25 2012-12-19 巴斯夫欧洲公司 次膦酸盐和硝酰基衍生物的阻燃剂组合物
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JP5654397B2 (ja) * 2011-03-25 2015-01-14 株式会社Adeka 太陽電池用封止膜
KR101505241B1 (ko) * 2012-03-16 2015-03-23 (주)엘지하우시스 Ｐｖｃ 무독 창호용 합성수지 조성물 및 ｐｖｃ 무독 창호
KR102092042B1 (ko) 2013-01-24 2020-03-24 삼성디스플레이 주식회사 액정 표시 장치 및 이의 제조 방법
CN103255491B (zh) * 2013-05-31 2015-05-20 中国科学院长春应用化学研究所 聚酰亚胺纤维的制备方法
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US11807753B2 (en) * 2020-10-28 2023-11-07 Cpk Interior Products Inc. Thermoplastic polyolefin-based slush powder compositions
JP2022187678A (ja) * 2021-06-08 2022-12-20 コニカミノルタ株式会社 樹脂組成物及びその製造方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1230293A (fr) * 1968-05-13 1971-04-28
EP1342748A1 (fr) * 2002-03-04 2003-09-10 Ciba SC Holding AG Combinaisons synergétiques d' absorbants UV pour des polyoléfines pigmentées
US20050192385A1 (en) * 2000-12-12 2005-09-01 Zurg Zingg Weatherability of flame retardant polyolefin

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4708979A (en) * 1985-05-02 1987-11-24 Ciba-Geigy Corporation Process for the stabilization of spherically polymerized polyolefins
US5283367A (en) * 1989-08-30 1994-02-01 Ciba-Geigy Corporation Substituted 1,4-diamino-2-butene stabilizers
EP0598005A1 (fr) 1991-08-05 1994-05-25 Eastman Chemical Company Composition de revetement aqueuse
EP0719826B1 (fr) * 1994-12-27 2001-09-12 SOLVAY POLYOLEFINS EUROPE - BELGIUM (Société Anonyme) Composition de polymère éthylénique
US6362258B1 (en) * 1995-12-29 2002-03-26 General Electric Company Stabilized thermoplastic polymer composition
US5968485A (en) 1998-10-16 1999-10-19 The Procter & Gamble Company UV protection compositions
DE10129231A1 (de) * 2001-06-19 2003-01-02 Basf Ag Stabilisierte thermoplastische Formmassen
CO5410180A1 (es) * 2002-10-22 2004-06-30 Ciba Sc Holding Ag Composicion y proceso para potenciar la produccion de bio-masa en invernaderos

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1230293A (fr) * 1968-05-13 1971-04-28
US20050192385A1 (en) * 2000-12-12 2005-09-01 Zurg Zingg Weatherability of flame retardant polyolefin
EP1342748A1 (fr) * 2002-03-04 2003-09-10 Ciba SC Holding AG Combinaisons synergétiques d' absorbants UV pour des polyoléfines pigmentées

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI427069B (zh) * 2007-12-03 2014-02-21 Ciba Holding Inc ２－（４，６－雙聯苯－４－基－１，３，５－三－２－基）－５－（２－乙基－（正）－己氧基）酚的晶形
WO2009071475A1 (fr) * 2007-12-03 2009-06-11 Basf Se Forme cristalline du 2-(4,6-bis-biphényl-4-yl-1,3,5-triazin-2-yl)-5-(2-éthyl-(n)-hexyloxy)phénol
AU2008333325B2 (en) * 2007-12-03 2013-05-02 Basf Se Crystalline form of 2-(4,6-bis-biphenyl-4-yl-1,3,5-triazin-2-yl)-5-(2-ethyl-(n)-hexyloxy)phenol
US8518503B2 (en) 2007-12-03 2013-08-27 Basf Se Crystalline form of 2-(4,6-bis-biphenyl-4-yl-1,3,5-triazin-2-yl)-5-(2-ethyl-(n)-hexyloxy)phenol
CN101939305B (zh) * 2007-12-03 2013-08-07 巴斯夫欧洲公司 2-(4，6-双-联苯-4-基-1，3，5-三嗪-2-基)-5-(2-乙基-(n)-己基氧基)酚的晶形
US8105668B2 (en) 2007-12-03 2012-01-31 Basf Se Crystalline form of 2-(4,6-bis-biphenyl-4-yl-1,3,5-triazin-2-yl)-5-(2-ethyl-(n)-hexyloxy)phenol
KR101587295B1 (ko) 2007-12-03 2016-01-21 바스프 에스이 2-(4,6-비스-바이페닐-4-일-1,3,5-트리아진-2-일)-5-(2-에틸-(ｎ)-헥실옥시)페놀의 결정형
KR20100103527A (ko) * 2007-12-03 2010-09-27 바스프 에스이 2-(4,6-비스-바이페닐-4-일-1,3,5-트리아진-2-일)-5-(2-에틸-(ｎ)-헥실옥시)페놀의 결정 형태
WO2009135813A1 (fr) * 2008-05-07 2009-11-12 Basf Se Matériau dégradable
US7947768B2 (en) 2009-03-02 2011-05-24 Saudi Arabian Oil Company Ultraviolet (UV) radiation stability and service life of woven films of polypropylene (PP) tapes for the production of jumbo bags
WO2010101732A1 (fr) * 2009-03-02 2010-09-10 Saudi Arabian Oil Company Stabilité améliorée vis-à-vis du rayonnement ultraviolet (uv) et durée de service améliorée de films tissés de bandes de polypropylène (pp) pour la production de gros sacs
WO2011020762A1 (fr) 2009-08-18 2011-02-24 Basf Se Module photovoltaïque uv-stabilisé
US20110237715A1 (en) * 2010-03-25 2011-09-29 Basf Se Flame retardant compositions of phosphinic acid salts and nitroxyl derivatives
CN101864109A (zh) * 2010-06-02 2010-10-20 王锦江 一种bopp薄膜用的复合型爽滑母料及其生产工艺
CN101864109B (zh) * 2010-06-02 2012-07-25 王锦江 一种bopp薄膜用的复合型爽滑母料及其生产工艺
EP2634296B1 (fr) 2010-10-29 2015-12-02 Dow Global Technologies LLC Bandes orientés, à base de polyéthylène et procédé de préparation associé
US9543521B2 (en) 2011-11-15 2017-01-10 Basf Se Organic semiconductor device and process for its production
WO2013152100A1 (fr) 2012-04-04 2013-10-10 Cytec Technology Corp. Polyoléfines stabilisées présentant une résistance accrue aux produits agrochimiques et aux uv et procédés d'utilisation
EP2647664A1 (fr) 2012-04-04 2013-10-09 Cytec Technology Corp. Procédé de stabilisation de films polyoléfiniques contre la dégradation par UV
CN109467903A (zh) * 2018-10-30 2019-03-15 惠州市中海源新材料科技有限公司 一种充电桩用聚碳酸酯组合物
CN109467903B (zh) * 2018-10-30 2020-12-08 惠州市中海源新材料科技有限公司 一种充电桩用聚碳酸酯组合物

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MX2008009972A (es) 2008-08-14
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BRPI0707359A8 (pt) 2018-04-03
CN101379122A (zh) 2009-03-04
KR20080094670A (ko) 2008-10-23
MA30219B1 (fr) 2009-02-02
ECSP088659A (es) 2008-09-29
BRPI0707359A2 (pt) 2011-05-03
EP1979406B1 (fr) 2012-10-24
BRPI0707359B1 (pt) 2018-10-09
MX304143B (es) 2012-10-09
CN101379122B (zh) 2012-09-26
US20100222471A1 (en) 2010-09-02
PT1979406E (pt) 2013-01-28
CA2636831C (fr) 2014-08-12
CA2636831A1 (fr) 2007-08-09
JP5308165B2 (ja) 2013-10-09
ZA200805900B (en) 2009-10-28
TW200740900A (en) 2007-11-01
IL192789A0 (en) 2009-02-11
KR101368176B1 (ko) 2014-03-14
US8173728B2 (en) 2012-05-08
JP2009525370A (ja) 2009-07-09

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